Shao Zhen, Liu Baolin, Peng Qinjian, Liu Wenge, Liu Yanpu, Liu Ruifeng, Xu Yongcheng, Liu Ling
Department of Traumatic and Aesthetic Surgery, Huangsi Aesthetic Surgery Hospital, 9 Huangsi Street, Beijing 100011, People's Republic of China.
Plast Reconstr Surg. 2007 Feb;119(2):500-7. doi: 10.1097/01.prs.0000246374.53516.78.
The purpose of this study was to investigate whether injections of marrow-derived mesenchymal progenitor cells could be used to facilitate new bone formation during distraction osteogenesis.
Fifteen New Zealand rabbits underwent bilateral osteotomy. After a 1-week latency period, bone distraction was activated at a rate of 2.0 mm/day for 5 days. The marrow-derived mesenchymal progenitor cells derived from the ilium marrow were cultured to a population of 10 in 0.5 ml and then unilaterally transplanted to the gap of distracted callus immediately after distraction had been terminated. Rabbits were killed at 2, 4, and 6 weeks after completion of bone lengthening. The distracted areas were harvested and evaluated by histologic, histomorphometric, radiographic, and scanning electron microscopic analysis. Bone mineral density in the lengthened callus was evaluated using dual-energy x-ray absorptiometry.
Radiographic evaluation indicated a significant increase in bony union of the distraction regenerate in the experimental side compared with the control side. Corresponding to the radiographic findings, the histologic examination showed an earlier and more intensive bone formation in the experimental side after 2, 4, and 6 weeks compared with the control side. Larger chondroid islands were found evident in distracted bone of the control side than in the experimental side.
The results show that transplantation of osteoblast-like cells promotes maturity of the distracted callus, as observed on the second and fourth weeks after lengthening. The method appears promising as a means of shortening the consolidation period of osteodistraction and decreasing complications during bone lengthening.
本研究的目的是探讨注射骨髓来源的间充质祖细胞是否可用于促进牵张成骨过程中的新骨形成。
15只新西兰兔接受双侧截骨术。经过1周的延迟期后,以每天2.0毫米的速度激活骨牵张,持续5天。将从髂骨髓中获取的骨髓来源的间充质祖细胞培养至10个细胞群体,置于0.5毫升培养基中,然后在牵张结束后立即将其单侧移植到牵张骨痂的间隙中。在骨延长完成后的第2、4和6周处死兔子。收集牵张区域并通过组织学、组织形态计量学、放射学和扫描电子显微镜分析进行评估。使用双能X线吸收法评估延长骨痂中的骨密度。
放射学评估表明,与对照侧相比,实验侧牵张再生的骨愈合有显著增加。与放射学结果相对应,组织学检查显示,与对照侧相比,实验侧在第2、4和6周后的骨形成更早且更密集。在对照侧牵张骨中发现的软骨样岛比实验侧更明显。
结果表明,如在延长后的第二周和第四周观察到的那样,移植成骨样细胞可促进牵张骨痂的成熟。该方法作为缩短骨牵张巩固期和减少骨延长过程中并发症的一种手段似乎很有前景。